Evidence map›Paper›PMID 19488400›Full record

ArticlePloS one2009

A novel protein isoform of the multicopy human NAIP gene derives from intragenic Alu SINE promoters.

Mark T Romanish, Hisae Nakamura, C Benjamin Lai, Yuzhuo Wang, Dixie L Mager

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  8. Broad detection of bacterial type III secretion system and flagellin proteins by the human NAIP/NLRC4 inflammasome.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  9. Structural variants caused byProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Review
  11. Article
  12. Article
  13. Salmonellae interactions with host processes.Nature reviews. Microbiology · 2015
    Review
  14. Epithelial NAIPs protect against colonic tumorigenesis.The Journal of experimental medicine · 2015
    Article
  15. Article
  16. Article
  17. Article
  18. Functional impact of the human mobilome.Current opinion in genetics & development · 2013
    Review
  19. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Mark T RomanishTerry Fox Laboratory, BC Cancer Agency, Vancouver, British Columbia, Canada.
Hisae Nakamura
C Benjamin Lai
Yuzhuo Wang
Dixie L Mager
BC Cancer Agency · CAUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human neuronal apoptosis inhibitory protein (NAIP) gene is no longer principally considered a member of the Inhibitor of Apoptosis Protein (IAP) family, as its domain structure and functions in innate immunity also warrant inclusion in the Nod-Like Receptor (NLR) superfamily. NAIP is located in a region of copy number variation, with one full length and four partly deleted copies in the reference human genome. We demonstrate that several of the NAIP paralogues are expressed, and that novel transcripts arise from both internal and upstream transcription start sites. Remarkably, two internal start sites initiate within Alu short interspersed element (SINE) retrotransposons, and a third novel transcription start site exists within the final intron of the GUSBP1 gene, upstream of only two NAIP copies. One Alu functions alone as a promoter in transient assays, while the other likely combines with upstream L1 sequences to form a composite promoter. The novel transcripts encode shortened open reading frames and we show that corresponding proteins are translated in a number of cell lines and primary tissues, in some cases above the level of full length NAIP. Interestingly, some NAIP isoforms lack their caspase-sequestering motifs, suggesting that they have novel functions. Moreover, given that human and mouse NAIP have previously been shown to employ endogenous retroviral long terminal repeats as promoters, exaptation of Alu repeats as additional promoters provides a fascinating illustration of regulatory innovations adopted by a single gene.

Indexed as

Promoter Regions, GeneticShort Interspersed Nucleotide ElementsAlu ElementsAnimalsDNA Transposable ElementsHeLa CellsHumansMiceNeuronal Apoptosis-Inhibitory ProteinNeuronsOpen Reading FramesProtein IsoformsProtein Structure, TertiaryRetroelementsRetroviridaeTissue DistributionDNA Transposable ElementsNAIP protein, humanNeuronal Apoptosis-Inhibitory ProteinProtein IsoformsRetroelements

Identifiers

PMID19488400
PMCPMC2685007
OpenAlexW2038624062

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.